Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/30083
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dc.contributor.authorZeybek, S.-
dc.contributor.authorTepeli, E.-
dc.contributor.authorÇetin, Gökhan Ozan-
dc.contributor.authorCaner, Vildan-
dc.contributor.authorŞenol, Hande-
dc.contributor.authorYildirim, B.-
dc.contributor.authorBağcı, Gülseren-
dc.date.accessioned2020-06-08T12:11:09Z
dc.date.available2020-06-08T12:11:09Z
dc.date.issued2019-
dc.identifier.issn1311-0160-
dc.identifier.urihttps://hdl.handle.net/11499/30083-
dc.identifier.urihttps://doi.org/10.2478/bjmg-2019-0002-
dc.description.abstractPentraxin 3 (PTX3), a prototypical member of the long pentraxin subfamily, is a evolutionarily conserved multimeric pattern recognition receptor involved in the humoral component of the innate immune system. Pentraxin 3 is released when tissue is stressed or damaged, and interacts with many different ligands. Pentraxin 3 exerts a pivotal role both as a regulator and as an indicator of inflammatory response in the pathogenesis of many diseases such as sepsis, vasculitis and preeclampsia. Uncontrolled inflammatory response is considered a major cause of unexplained recurrent pregnancy loss (URPL). We determined the PTX3 messenger ribonucleic acid (mRnA) and protein expression levels in placentai tissues from 50 women with URPL, and made comparison with those in 50 age-matched control subjects. In quantitative real-time polymerase chain reaction (qRT-PcR) and immunohistochemistry analyses, PTX3 mRnA and protein levels, respectively, were significantly increased in URPL patients compared with their respective controls (p = 0.0001). Although no significant correlations were identified between PTX3 expression levels and clinical parameters such as maternal age, numbers of previous pregnancy losses, and gestational age at miscarriage, PTX3 mRnA expression was significantly higher in patients with no live births than in women with previous live births (p = 0.0001). Our study suggests that tissue-specific expression of PTX3 is associated with URPL. Further larger studies are required to determine whether PTX3 expression can be used as a biomarker to manage URPL in routine clinical practice. © 2019 zeybek S, Tepeli E, cetin GO, caner V, Senol H, Yildirim B, Bagci G, published by Sciendo 2019.en_US
dc.language.isoenen_US
dc.publisherSciendoen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectInflammationen_US
dc.subjectPentraxin 3 (PTX3)en_US
dc.subjectPlacentai expressionen_US
dc.subjectReal-time polymerase chain reaction (RT-PCR)en_US
dc.subjectUnexplained recurrent pregnancy loss (URPL)en_US
dc.subjectmessenger RNAen_US
dc.subjectpentraxin 3en_US
dc.subjectArticleen_US
dc.subjectclinical articleen_US
dc.subjectcontrolled studyen_US
dc.subjectfemaleen_US
dc.subjectfetusen_US
dc.subjectgestational ageen_US
dc.subjecthumanen_US
dc.subjecthuman tissueen_US
dc.subjectimmunohistochemistryen_US
dc.subjectlive birthen_US
dc.subjectmaternal ageen_US
dc.subjectmedically unexplained symptomen_US
dc.subjectplacenta tissueen_US
dc.subjectprotein expressionen_US
dc.subjectprotein expression levelen_US
dc.subjectreal time polymerase chain reactionen_US
dc.subjectrecurrent abortionen_US
dc.titleIncreased expression of pentraxin 3 in placental tissues from patients with unexplained recurrent pregnancy lossen_US
dc.typeArticleen_US
dc.identifier.volume22en_US
dc.identifier.issue1en_US
dc.identifier.startpage21
dc.identifier.startpage21en_US
dc.identifier.endpage28en_US
dc.identifier.doi10.2478/bjmg-2019-0002-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.pmid31523616en_US
dc.identifier.scopus2-s2.0-85072379651en_US
dc.identifier.wosWOS:000483955200003en_US
dc.identifier.scopusqualityQ4-
dc.ownerPamukkale University-
item.openairetypeArticle-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextWith Fulltext-
item.grantfulltextopen-
item.cerifentitytypePublications-
crisitem.author.dept14.02. Internal Medicine-
crisitem.author.dept14.02. Internal Medicine-
crisitem.author.dept14.03. Basic Medical Sciences-
crisitem.author.dept14.02. Internal Medicine-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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